Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractReclamation of treated domestic wastewater using biological membrane assisted carbon filtration (BioMAC)    Next AbstractTunnel entries and a killing agent uncover the importance of fly retention in Drosophila suzukii traps »

J Mol Biol


Title:The Saccharomyces cerevisiae homologue YPA1 of the mammalian phosphotyrosyl phosphatase activator of protein phosphatase 2A controls progression through the G1 phase of the yeast cell cycle
Author(s):Van Hoof C; Janssens V; De Baere I; de Winde JH; Winderickx J; Dumortier F; Thevelein JM; Merlevede W; Goris J;
Address:"Afdeling Biochemie, Faculteit Geneeskunde, Katholieke Universiteit Leuven, Herestraat 49, Leuven, B-3000, Belgium"
Journal Title:J Mol Biol
Year:2000
Volume:302
Issue:1
Page Number:103 - 120
DOI: 10.1006/jmbi.2000.4062
ISSN/ISBN:0022-2836 (Print) 0022-2836 (Linking)
Abstract:"The Saccharomyces cerevisiae gene YPA1 encodes a protein homologous to the phosphotyrosyl phosphatase activator, PTPA, of the mammalian protein phosphatase type 2A (PP2A). In order to examine the biological role of PTPA, we disrupted YPA1 and characterised the phenotype of the ypa1Delta mutant. Comparison of the growth rate of the wild-type strain and the ypa1Delta mutant on glucose-rich medium after nutrient depletion showed that the ypa1Delta mutant traversed the lag period more rapidly. This accelerated progression through 'Start' was also observed after release from alpha-factor-induced G1 arrest as evidenced by a higher number of budding cells, a faster increase in CLN2 mRNA expression and a more rapid reactivation of Cdc28 kinase activity. This phenotype was specific for deletion of YPA1 since it was not observed when YPA2, the second PTPA gene in budding yeast was deleted. Reintroduction of YPA1 or the human PTPA cDNA in the ypa1Delta mutant suppressed this phenotype as opposed to overexpression of YPA2. Disruption of both YPA genes is lethal, since sporulation of heterozygous diploids resulted in at most three viable spores, none of them with a ypa1Delta ypa2Delta genotype. This observation indicates that YPA1 and YPA2 share some essential functions. We compared the ypa1Delta mutant phenotype with a PP2A double deletion mutant and a PP2A temperature-sensitive mutant. The PP2A-deficient yeast strain also showed accelerated progression through the G1 phase. In addition, both PP2A and ypa1Delta mutants show similar aberrant bud morphology. This would support the notion that YPA1 may act as a positive regulator of PP2A in vivo"
Keywords:"CDC28 Protein Kinase, S cerevisiae/metabolism *Cell Cycle/drug effects Cyclins/genetics Flow Cytometry Fungal Proteins/genetics G1 Phase/drug effects Gene Deletion Gene Expression Regulation, Fungal/drug effects Genes, Fungal/genetics Glucose/metabolism H;"
Notes:"MedlineVan Hoof, C Janssens, V De Baere, I de Winde, J H Winderickx, J Dumortier, F Thevelein, J M Merlevede, W Goris, J eng Research Support, Non-U.S. Gov't Netherlands 2000/08/31 J Mol Biol. 2000 Sep 8; 302(1):103-20. doi: 10.1006/jmbi.2000.4062"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024